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HYLS1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Analysis of the Indacaterol-Regulated Transcriptome in Human Airway
Chloride Channels Regulate Differentiation and Barrier Functions
Systematic Analysis of Palatal Transcriptome to Identify Cleft Palate Genes Within Tgfβ3-Knockout Mice Alleles: RNA-Seq Analysis of Tgfβ3 Mice Ozturk Et Al
Based on Network Pharmacology and RNA Sequencing Techniques to Explore the Molecular Mechanism of Huatan Jiangzhuo Decoction for Treating Hyperlipidemia
Whole-Exome Sequencing Identifies Causative Mutations in Families
The Molecular Basis of Hydrolethalus Syndrome
Supplemental Data.Pdf
Discovery, Diagnosis, and Etiology of Craniofacial Ciliopathies
THE IMPORTANT ROLE of GENETIC SCREENING Making the Best Decisions for You and Your Family
Novel Mutations for Nonsyndromic Cleft Lip and Palate in Two Consanguineous Palestinian Families
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Table of Contents
Mouse Ddx25 Conditional Knockout Project (CRISPR/Cas9)
Computational Study of Hydrolethalus Syndrome: D211G Mutation Destabilizes the Structural Stability of HYLS1 Leading to the Formation of Nuclear Inclusions Paul M
Recurrence Risks for Different Pregnancy Outcomes and Meiotic Segregation Analysis of Spermatozoa in Carriers of T(1;11)(P36.22;Q12.2)
Structural Analysis of the Genome of Breast Cancer Cell Line ZR-75-30
Mechanism and Regulation of Centriole and Cilium Biogenesis
Top View
Network Analysis Identifies Mitochondrial Regulation Of
Use of Multivariate Discriminant Methodologies in the Analysis of Phenotypic and Genomic Data of Cattle
The Hydrolethalus Syndrome Protein HYLS-1 Links Core Centriole Structure to Cilia Formation
Update on Pathogenesis of Primary Adrenal Insufficiency: Beyond Steroid Enzyme Deficiency and Autoimmune Adrenal Destruction
New Insight Into Human Ciliopathy 4 August 2009
Human Embryonic Expression Identifies Novel Essential Gene Candidates
In-Silico Guided Identification of Ciliogenesis Candidate Genes in a Non-Conventional Animal Model
The Molecular Basis of Hydrolethalus Syndrome